Legionella selective agar (UDI 08594199921106)
Manufactured by VIAMAR INTERNATIONAL, s.r.o.
Device Regulatory Overview
The Legionella selective agar (Model/Catalog Number: 98224-10) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98224-10
- Product Code / EMDN
- W0104010405
- Device Name
- Legionella selektivní agar
- Database Sync Date
- 2026-08-09 16:47:58
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Legionella selective agar?
The registered manufacturer of record for Legionella selective agar is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for Legionella selective agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199921106.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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